| 2026-09-09 | FDA Drug | FDA Recall: Famotidine Injection in Sodium Chloride Injection, 20 mg, 50 mL in GALAXY Single Dose Container, Rx | Baxter Healthcare Corporation | Class II | N/A |
| 2026-09-09 | FDA Drug | FDA Recall: Clindamycin Phosphate in 0.9% Sodium Chloride Injection, 600 mg per 50 mL (12 mg/mL), 50 mL Single-D | Baxter Healthcare Corporation | Class II | N/A |
| 2026-09-09 | FDA Device | FDA Recall: Baxter Novum IQ Syringe Pump, Model Number 40800BAXUS | Baxter Healthcare Corporation | Class II | N/A |
| 2026-09-09 | FDA Drug | FDA Recall: CARDENE IV (Nicardipine Hydrochloride) in 0.83% Sodium Chloride Injection, 40 mg in 200 mL (0.2 mg/m | Baxter Healthcare Corporation | Class II | N/A |
| 2026-09-09 | FDA Device | FDA Recall: Baxter Novum IQ Syringe Pump, Loaner, Model Number 40800BAXUSL | Baxter Healthcare Corporation | Class II | N/A |
| 2026-09-09 | FDA Drug | FDA Recall: Vasopressin, in 0.9% Sodium Chloride Injection, 20 units per 100 mL (0.2 units/mL), 100mL Single-Dos | Baxter Healthcare Corporation | Class II | N/A |
| 2026-09-09 | FDA Drug | FDA Recall: Clindamycin Injection USP in 5% Dextrose, 900 mg per 50 mL (12 mg/mL) in GALAXY 50 mL Single Dose Co | Baxter Healthcare Corporation | Class II | N/A |
| 2026-09-09 | FDA Drug | FDA Recall: Clindamycin Injection USP in 5% Dextrose, 900 mg/50 mL (18 mg/mL), in GALAXY 50 mL Single Dose Conta | Baxter Healthcare Corporation | Class II | N/A |
| 2026-09-09 | FDA Drug | FDA Recall: Vancomycin Injection, USP, in 0.9% Sodium Chloride, 1g per 200 mL (5 mg/mL) in GALAXY Single-Dose Co | Baxter Healthcare Corporation | Class II | N/A |
| 2026-09-09 | FDA Drug | FDA Recall: Daptomycin, in 0.9% Sodium Chloride Injection, 500 mg per 50 mL (10 mg/mL), 500 mg total, in 50 mL S | Baxter Healthcare Corporation | Class II | N/A |
| 2026-09-09 | FDA Drug | FDA Recall: Daptomycin, in 0.9% Sodium Chloride Injection, 1,000 mg per 100 mL (10 mg/mL), 1,000 mg total, in 10 | Baxter Healthcare Corporation | Class II | N/A |
| 2026-09-09 | FDA Drug | FDA Recall: Clindamycin Injection USP in 5% Dextrose, 600 mg per 50 mL (12 mg/mL) in GALAXY 50 mL Single Dose Co | Baxter Healthcare Corporation | Class II | N/A |
| 2026-09-09 | FDA Drug | FDA Recall: Vasopressin, in 0.9% Sodium Chloride Injection, 40 units per 100 mL (0.4 units/mL), 100mL Single-Dos | Baxter Healthcare Corporation | Class II | N/A |
| 2026-09-09 | FDA Drug | FDA Recall: Vancomycin Injection, USP in 5% Dextrose, 1 g per 200mL (5 mg/mL), in GALAXY Single-Dose Container, | Baxter Healthcare Corporation | Class II | N/A |
| 2026-09-09 | FDA Drug | FDA Recall: MYXREDLIN, Insulin Human in 0.9% Sodium Chloride Injection, 100 units/100 mL (1 unit/mL), Rx only, B | Baxter Healthcare Corporation | Class II | N/A |
| 2026-09-09 | FDA Drug | FDA Recall: Pantoprazole Sodium in 0.9% Sodium Chloride Injection, 80 mg/100 mL (0.8 mg/mL) Single-Dose Infusion | Baxter Healthcare Corporation | Class II | N/A |
| 2026-09-09 | FDA Drug | FDA Recall: Nexterone (amiodarone HCI), 360 mg/200 mL (1.8 mg/mL) in GALAXY Single-Dose Container, sterile, Nonp | Baxter Healthcare Corporation | Class II | N/A |
| 2026-09-09 | FDA Drug | FDA Recall: Dexmedetomidine Hydrochloride in 0.9% Sodium Chloride Injection, 400 mcg per 100 mL (4 mcg/mL) in Ga | Baxter Healthcare Corporation | Class II | N/A |
| 2026-09-09 | FDA Drug | FDA Recall: Clindamycin Injection USP in 5% Dextrose, 900 mg/50 mL (18 mg/mL), in GALAXY 50 mL Single Dose Conta | Baxter Healthcare Corporation | Class II | N/A |
| 2026-08-19 | FDA Device | FDA Recall: Baxter Duo-Vent Solution Set and Male Luer Lock Adapter, Product Code 1C8507; Solution Administratio | Baxter Healthcare Corporation | Class I | N/A |
| 2026-07-08 | FDA Device | FDA Recall: Hillrom VOLARA System P.CIRCUIT 5KIT AC, (Single Patient Use Circuit), Model/Catalog Number REF M084 | Baxter Healthcare Corporation | Class I | N/A |
| 2026-07-08 | FDA Device | FDA Recall: Adapter for Head Positioning, Model/Catalog Number: 1739994, when used in conjunction with the side | Baxter Healthcare Corporation | Class II | N/A |
| 2026-07-08 | FDA Device | FDA Recall: Hillrom VOLARA System P.CIRCUIT KIT (Single Patient Use Circuit), Model/Catalog Number REF M08085; O | Baxter Healthcare Corporation | Class I | N/A |
| 2026-07-08 | FDA Device | FDA Recall: Hillrom VOLARA P.CIRCUIT 5KIT (System Single Patient Use Circuit), Model/Catalog Number REF M08270; | Baxter Healthcare Corporation | Class I | N/A |
| 2026-07-08 | FDA Device | FDA Recall: Hillrom VOLARA System P.CIRCUIT KIT AC (Single Patient Use Circuit), Model/Catalog Number REF M08473 | Baxter Healthcare Corporation | Class I | N/A |
| 2026-06-10 | FDA Device | FDA Recall: Brand Name: Exacta Mix Product Name: Vented Micro-Volume Inlet Model/Catalog Number: H938175 P | Baxter Healthcare Corporation | Class II | N/A |
| 2026-04-08 | FDA Device | FDA Recall: Blue Ventilator Adapter Module, single-patient use circuit, Product Code M07937. Accessory to Baxte | Baxter Healthcare Corporation | Class I | N/A |
| 2026-03-25 | FDA Device | FDA Recall: Brand Name: Welch Allyn, Inc. Product Name: Welch Allyn Spot Vision Screener VS100 Model/Catalog N | Baxter Healthcare Corporation | Class II | N/A |